Institute of Tropical Medicine and International Health, Charité- Universitätsmedizin Berlin, Germany.
Kuala Kencana Clinic, PT Freeport Indonesia/International SOS, Papua, Indonesia.
PLoS One. 2019 Feb 25;14(2):e0212432. doi: 10.1371/journal.pone.0212432. eCollection 2019.
Papua Province, Indonesia is experiencing an on-going epidemic of Human Immunodeficiency Virus (HIV) infection, with an estimated 9-fold greater prevalence than the overall national rate. This study reviewed the treatment outcomes of an HIV-infected cohort on Antiretroviral Therapy (ART) and the predictors in terms of immunological recovery and virological response.
ART-naïve individuals in a workplace HIV program in southern Papua were retrospectively analyzed. Patients were assessed at 6, 12 and 36 months after ART initiation for treatment outcomes, and risk factors for virological suppression (viral load (VL) <1,000 copies/ml), poor immune response (CD4 <200 cells/mm3) and immunological failure (CD4 <100 cells/ mm3) after at least 6 months on ART, using a longitudinal Generalized Estimating Equations multivariate model.
Assessment of 105 patients were included in the final analysis with a median age of 34 years, 88% male, median baseline CD4 236 cells/ mm3, and VL 179,000 copies/ml. There were 74, 73, and 39 patients at 6, 12, and 36 months follow-up, respectively, with 5 deaths over the entire period. For the three observation periods, 68, 80, and 75% of patents achieved virological suppression, poor immune responders decreased from 15, 16 to 10%, whilst 15, 16, 10% met the immunological failure criteria, respectively. Using multivariate analysis, the independent predictor for viral suppression at 12 and 36 months was ≥1 log decrease in VL at 6 months (OR 19.25, p<0.001). Higher baseline CD4 was significantly correlated with better immunological outcomes, and lower likelihood of experiencing immunological failure (p <0.001).
Virological response at six months after beginning ART is the strongest predictor of viral suppression at 12 and 36 months, and may help in identifying patients needing additional adherence therapy support. Higher baseline CD4 positively affects the immunological outcomes of patients. The findings indicate HIV control programs should prioritize the availability of VL testing and begin ART regardless of CD4 counts in infected patients.
印度尼西亚巴布亚省正经历着一场人免疫缺陷病毒(HIV)感染的持续流行,其流行率比全国平均水平高出约 9 倍。本研究回顾了接受抗逆转录病毒治疗(ART)的 HIV 感染队列的治疗结果,以及在免疫恢复和病毒学应答方面的预测因素。
对巴布亚南部工作场所 HIV 项目中的 ART 初治个体进行回顾性分析。患者在开始 ART 后 6、12 和 36 个月时进行评估,以了解治疗结果,以及在开始 ART 至少 6 个月后病毒学抑制(病毒载量(VL)<1,000 拷贝/ml)、免疫应答不良(CD4<200 个细胞/mm3)和免疫失败(CD4<100 个细胞/mm3)的预测因素,使用纵向广义估计方程多变量模型。
最终纳入 105 例患者进行了最终分析,中位年龄为 34 岁,88%为男性,中位基线 CD4 为 236 个细胞/mm3,VL 为 179,000 拷贝/ml。分别有 74、73 和 39 例患者在 6、12 和 36 个月时进行了随访,整个研究期间有 5 例死亡。在三个观察期内,68%、80%和 75%的患者达到了病毒学抑制,免疫应答不良患者从 15%、16%减少至 10%,而免疫失败的患者分别为 15%、16%和 10%。多变量分析表明,6 个月时 VL 下降≥1 对数是 12 个月和 36 个月时病毒学抑制的独立预测因素(OR 19.25,p<0.001)。较高的基线 CD4 与更好的免疫结果显著相关,降低了发生免疫失败的可能性(p<0.001)。
开始 ART 后 6 个月时的病毒学反应是 12 个月和 36 个月时病毒学抑制的最强预测因素,可能有助于识别需要额外依从性治疗支持的患者。较高的基线 CD4 对患者的免疫结果有积极影响。研究结果表明,HIV 控制项目应优先考虑提供 VL 检测,并开始无论 CD4 计数如何都应开始 ART。